Psephos Biomedica and SEHTA are excited to present a briefing webinar covering key regulatory topics for medical devices in Digital Health, AI and IVD technology.
Date: Thursday 20th January 2022
Times: 10:00 – 11:00 (GMT)
Cost: Free of charge
This briefing session has been designed to help you update your knowledge, improve your skillset, and move your medical technologies and companies forward.
After the significant events of the last two years 2022 is poised to be a year of further growth in the medical technology field and, with it, increased regulations and related compliance needs. This briefing session is designed to give you an update on the major topics you need to consider as we go into the year, the key actions that you need to take to meet the challenges ahead, and an awareness of areas that you need to explore further.
Inventors, entrepreneurs and manufacturers wanting to access the UK or EU medical technology market. All Medical Technology Entrepreneurs, Medical Device Software Developers, Technology Transfer Officers, Medical Technology University Researchers, IVD Developers, Business Owners, Executives, Product Owners and Regulatory Specialists within a company that need to understand the overall regulatory requirements for their medical devices to enable them to place a device on the market and to maintain access. All company sizes will find it useful.